nuclear type mitochondrial complex I deficiency 8

Summary
Synonym
  • MC1DN8
Definition
A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS3 gene on chromosome 11p11.2.
Super Class
autosomal recessive disease nuclear type mitochondrial complex I deficiency
Disease Ontology
DOID:0112081
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4722 NDUFS3 NADH:ubiquinone oxidoreductase core subunit S3

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024